Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development-Reference-Cited by-同舟云学术

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Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development

Published:2015-07 Issue: Volume:130 Page:1-28
ISSN:0301-0082
Container-title:Progress in Neurobiology
language:en
Short-container-title:Progress in Neurobiology

Author:

Meechan Daniel W.,Maynard Thomas M.,Tucker Eric S.,Fernandez Alejandra,Karpinski Beverly A.,Rothblat Lawrence A.,LaMantia Anthony-S.

Funder

National Institute of Child Health and Human Development

NIDCD

NICHD

Simons Foundation

NARSAD Young Investigator

Publisher

Elsevier BV

Subject

General Neuroscience

Reference310 articles.

1. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons;Albrecht;Nat. Genet.,1997

2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

3. Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome;Andersson;Biol. Psychiatry,2008

4. Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors;Andreassen;Am. J. Hum. Genet.,2013

5. Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion);Antshel;J. Autism Dev. Disord.,2007

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